A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602833



Internal ID16043556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33567103..33620370hg38UCSC Ensembl
Innerchr6:33534880..33588147hg19UCSC Ensembl
Innerchr6:33642858..33696125hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3853268
hg1953268
hg1853268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1057646
Samples
Known GenesBAK1, GGNBP1, LINC00336
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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